期刊文献+

多节段髓内先天性肿瘤和良性室管膜瘤的对比分析 被引量:2

Comparative analysis between multi-segments intramedullary spinal cord congenital tumors and benign ependymomas
下载PDF
导出
摘要 目的:对比分析多节段髓内先天性肿瘤和良性室管膜瘤患者在性别、年龄分布,以及肿瘤部位、瘤体长度、切除程度和对围手术期神经功能状况影响方面的异同。方法:选取北京大学第三医院近8年来连续收治的12例多节段(≥3个椎体节段)髓内先天性肿瘤和19例良性室管膜瘤患者,均行后正中入路显微镜下肿瘤切除术。收集患者临床资料,将二便功能状态分为4级(正常,尿频或/和便秘等轻度异常,排便困难、无力等中度异常,失禁),以改良JOA评分系统(improved Japanese orthopaedic association score system,IJOA)评价神经功能状况,以IJOA分值差(术后IJOA和术前IJOA差值)评估手术效果。所有患者随访至2009年6月30日。以独立样本的t检验和非参数检验分析统计学数据。结果:先天性肿瘤患者的平均年龄为(23.5±14.3)岁,良性室管膜瘤患者为(37.8±12.9)岁,差异有统计学意义(t=-2.89,P=0.007)。两组性质不同的多节段髓内肿瘤比较,其肿瘤部位(Z=-3.59,P=0.001)和肿瘤切除程度(Z=-2.89,P=0.004)差异均有统计学意义。83.3%(10/12)患者的多节段髓内先天性肿瘤累及脊髓圆锥部位,部分肿瘤和脊髓结构粘连紧密或脂肪组织穿插生长在神经结构中,为避免神经功能的缺失,不能强行切除粘连紧密的肿瘤组织,其中66.7%(8/12)肿瘤组织得以全部切除或近乎全部切除。78.9%(15/19)患者的多节段髓内良性室管膜瘤累及颈段或颈胸段脊髓,其中94.7%(18/19)肿瘤组织得以全部切除或近乎全部切除。结论:多节段髓内先天性肿瘤可能多见于青年患者,常累及脊髓圆锥,部分肿瘤全部切除难度较大;多节段髓内良性室管膜瘤可能多见于中年患者,常累及颈段或颈胸段脊髓,肿瘤全部切除较容易。 Objective:To comparatively analyze the different and common points between multi-segments intramedullary spinal cord congenital tumors and benign ependymomas,such as the patient's age,gender,nervous functions and tumor location,longitudinal extension,and removed extent.Methods: Data were studied from 12 patients with multi-segments intramedullary spinal cord congenital tumors and 19 patients with multi-segments intramedullary spinal cord benign ependymomas who underwent microsurgery for the tumor using a posterior approach.The tumor was exposed through dorsal myelotomy.Preoperative and postoperative nervous functions were scored using the Improved JOA(improved Japanese orthopaedic association,IJOA) score system.Independent sample t-test was performed for ages,preoperative IJOA scores,postoperative IJOA scores and IJOA difference values of the patients,and longitudinal extension of tumors in the two groups with congenital tumors and benign ependymomas.Two independent sample Mann-Whitney tests was performed for the patient's gender,stool and urine functions,limbs weakness,and tumor removed extent in the two groups.All patients were followed-up until Jun.30,2009.Results: The average age of patients in congenital tumors group was 23.5±14.3,and in benign ependymomas group was 37.8±12.9,the age difference between the two groups was statistically significant(t=-2.89,P=0.007).The difference for location(Z=-3.59,P=0.001)and removed extent(Z=-2.89,P=0.004) of tumors between the two groups was statistically significant.Those located at the conus accounted for almost 83.3%(10/12)multi-segments intramedullary spinal cord congenital tumors.Because of the stiff adhesion with adjacent neural structures or penetrative growth in surrounding spinal marrow,some congenital tumors could not totally removed by force.The main purpose of surgery for these tumors was not total removal but decompression on the adjacent neural structures.Total or nearly total resection was achieved in 66.7%(8/12)patients diagnosed with congenital tumors.78.9(15/19)percent of multi-segments intramedullary spinal cord benign ependymomas were located at the cervical and cervicothoracic segments.Total or nearly total resection was achieved in 94.7%(18/19)patients with benign ependymomas.Conclusion: It is known from the clinical files that most multi-segments intramedullary spinal cord congenital tumors are found in young patients and most benign ependymomas in the middle-aged.Most congenital tumors are located at the conus,and they are difficult to totally remove.Most benign ependymomas are located at the cervical and cervicothoracic segments,and they are easy to totally remove.
出处 《北京大学学报(医学版)》 CAS CSCD 北大核心 2010年第2期183-187,共5页 Journal of Peking University:Health Sciences
关键词 脊髓肿瘤 室管膜瘤 对比研究 Spinal cord neoplasms Ependymoma Comparative study
  • 相关文献

参考文献15

  • 1Sandalcioglu IE,Gasser T,Asori S,et al.Functional outcome after surgical treatment of intramedullary spinal cord tumors:expe-rience with 78 patients[J].Spinal Cord,2005,43(1):34-41.
  • 2PENG Lin QI Song-tao CHEN Zhuang FEN Wen-feng FANG Lu-xiong HUANG Li-jing CHENG Jiang-peng.Radical microsurgical treatment of intramedullary spinal cord tumors[J].Chinese Medical Journal,2006(16):1343-1347. 被引量:6
  • 3杨玉明,姜宏志,沙成,袁庆国,王长春,谢红雯,周昆,王大明.多节段颈髓室管膜瘤的手术治疗[J].中华外科杂志,2007,45(10):705-707. 被引量:3
  • 4Lin YH,Huang CI,Wong TT,et al.Treatment of spinal cord ependymomas by surgery with or without postoperative radiotherapy[J].J Neurooncol,2005,71(2):205-210.
  • 5Quigley DG,Farooqi N,Pigott TJ,et al.Outcome predictors in the management of spinal cord ependymoma[J].Eur Spine J,2007,16(10):399-404.
  • 6Sun Jianjun,Wang Zhenyu,Li Zhendong,et al.Microsurgical treatment and functional outcomes of multi-segment intramedullary spinal cord tumors[J].J Clin Neurosci,2009,16(5):666-671.
  • 7孙建军,王振宇,李振东,马长城,刘彬,赵继宗.影响多节段髓内良性肿瘤手术效果的相关因素分析[J].北京医学,2009,31(3):131-134. 被引量:3
  • 8Kasim KA,Thumher MM,Mekeever P,et al.Intradural spinal tumors:current classification and MRI features[J],Neurora-diology,2008,50(4):301-314.
  • 9王贵怀,杨俊,刘藏,韩波,李德志,陈思源,杨宝.脊髓髓内室管膜瘤的显微外科治疗——附173例临床总结[J].中国神经肿瘤杂志,2007,5(1):9-12. 被引量:19
  • 10Paterakis KN,Karantanas AH,Barbanis S,et al.Cervical spinal cord intramedullary teratoma[J].Clin Neurol Neurosurg,2006,108(5):514-517.

二级参考文献36

共引文献40

同被引文献22

  • 1景治涛,罗世祺,甲戈,马振宇,张玉琪.儿童脊髓内肿瘤的显微外科治疗[J].中华小儿外科杂志,2006,27(3):117-119. 被引量:2
  • 2杨玉明,姜宏志,沙成,袁庆国,王长春,谢红雯,周昆,王大明.多节段颈髓室管膜瘤的手术治疗[J].中华外科杂志,2007,45(10):705-707. 被引量:3
  • 3Sandalcioglu IE, Gasser T, Asgari S, et al. Functional outcome after surgical treatment of intramedullary spinal cord tumors: experience with 78 patients. Spinal Cord,2005,43:34-41.
  • 4Lin YH, Huang CI, Wong TT, et al. Treatment of spinal cord ependymomas by surgery with or without postoperative radiotherapy. J Neurooncol,2005,71:205-210.
  • 5Kim MS, Chung CK, Choe GY, et al. Intramedullary spinal cord astrocytoma in adults: postoperative outcome. J Neurooncol,2001,52: 85-94.
  • 6Nakamura M, Ishii K, Watanabe K, et al. Surgical treatment of intramedullary spinal cord tumors: prognosis and complications. Spinal Cord,2008,46:282-286,.
  • 7Sun JJ, Wang ZY, Li ZD, et al. Microsurgical treatment and functional outcomes of multi-segment intramedullary spinal cord tumors. J Clin Neurosci,2009,16:666-671.
  • 8Crawford JR, Zaninovic A, Santi M, et al. Primary spinal cord tumors of childhood : effects of clinical presentation, radiographic features, and pathology on survival. J Neurooncol, 2009, 95:259-269.
  • 9Wilson PE, Oleszek JL Clayton GH. Pediatric Spinal Cord Tumors and Masses. J Spinal Cord Med, 2007,30:S15-S20.
  • 10Sandler HM, Papadopoulos SM, Thornton AF, et al. Spinal cord astrocytomas: results of therapy. Neurosurgery, 1992, 30:490-493.

引证文献2

二级引证文献2

相关作者

内容加载中请稍等...

相关机构

内容加载中请稍等...

相关主题

内容加载中请稍等...

浏览历史

内容加载中请稍等...
;
使用帮助 返回顶部